Search the 13 jobs at Thermo Fisher Scientific

The Associate Research Scientist in Analytical Development will handle method development and execution of analytical techniques such as HPLC, UPLC, and GC to support drug product development. Responsibilities include characterizing processes and finished products, collaborating with project teams, and presenting results.

The Quality Specialist II role involves maintaining quality systems, ensuring compliance with medical device standards, managing non-conformances, and supporting audit processes. Key responsibilities include handling quality issues, managing controlled documents, conducting internal audits, and generating quality reports using various software applications.

The Assistant Scientist will conduct routine sample preparation and analysis of pharmaceutical and biopharmaceutical compounds under general supervision. Responsibilities include operating analytical instruments, maintaining documentation, and ensuring compliance with SOPs and regulatory guidelines. The role emphasizes accurate data review and communication of project status.

The Sr. Product Specialist in Life Sciences is responsible for sales of research products within a designated territory. Key tasks include maintaining customer relationships, developing sales strategies, introducing new products, and managing territory profitability. A strong technical background in life sciences and sales experience is essential for success in this role.

As Staff Program Manager, you will oversee the development and regulatory submission of Oncology Companion Diagnostic assays, manage program timelines and budgets, identify risks, and ensure compliance with product commercialization processes, acting as a key liaison with internal teams and external clients.

The Quality Assurance Supervisor at Thermo Fisher Scientific in San Jose is responsible for incoming inspections, material/instrument disposition processes, and Customer quality for Life Science Mass Spectrometry products. They lead quality initiatives, drive a robust First Article inspection program, and ensure product quality measures improve customer satisfaction.

The Senior Manager of Data Engineering will lead a team to manage data analytics IT infrastructure, ensuring alignment with business objectives. Responsibilities include overseeing data projects, maintaining scalable data pipelines, and implementing strategies for efficient data management, while also mentoring the team.

The Account Manager III will develop and manage key accounts in the Colombian market, implement growth strategies, maintain client relationships, and collaborate with internal teams to deliver exceptional service while adhering to company policies.

The Sr Quality Control Specialist is accountable for overseeing Technology Transfer of methods for new products, ensuring quality verification and daily testing to support Manufacturing Operations. The role requires resource management, QA oversight, and maintaining a strong quality culture while developing colleagues within the quality team.

Staff Automation Engineer with strong leadership and technical expertise in integrating complex systems. Responsibilities include training new engineers, fixing integrated systems, automating processes, leading projects, and ensuring smooth integration of new products.

The Scientist III - Technical Project Manager performs complex laboratory analysis of pharmaceutical products, leads multiple projects, and communicates regulatory issues. Responsibilities include method validation, analytical testing, data review, report writing, and mentoring team members while ensuring adherence to GMP and GLP standards.

The Senior Scientist will lead complex laboratory analyses involving pharmaceutical products, perform method validations, method transfers, and analytical testing while ensuring compliance with GMP standards. Responsibilities include project leadership, report writing, mentoring team members, and overseeing technical compliance.

The Scientist II - HPLC role involves performing complex sample preparation and analysis for pharmaceutical and biopharmaceutical compounds, adhering to quality and regulatory standards. Responsibilities include maintaining analytical instruments, training team members, problem-solving related to instrumentation, and analyzing data for compliance with industry protocols.